Unnatural cyclodextrins can be accessed from enzyme-mediated dynamic combinatorial libraries
Author:
Affiliation:
1. Department of Chemistry, Technical University of Denmark, Kongens Lyngby DK-2800, Denmark
2. Univ. Artois, CNRS, Centrale Lille, Univ. Lille, UMR 8181, Unité de Catalyse et Chimie du Solide (UCCS), Lens 62300, France
Abstract
Funder
Novo Nordisk Fonden
Carlsbergfondet
Villum Fonden
Publisher
Royal Society of Chemistry (RSC)
Subject
Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis
Link
http://pubs.rsc.org/en/content/articlepdf/2022/CC/D1CC06452E
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4. Enzymatic Generation and In Situ Screening of a Dynamic Combinatorial Library of Sialic Acid Analogues
5. Enzyme-mediated dynamic combinatorial chemistry allows out-of-equilibrium template-directed synthesis of macrocyclic oligosaccharides
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